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Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.

Primary Purpose

Inguinal Hernia

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Ultra sound guided nerve block
Usual infiltration
Sponsored by
Imam Abdulrahman Bin Faisal University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Inguinal Hernia

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers
  • Inclusion criteria:

    1. Patients who underwent elective inguinal hernia repair (will consider the hernia size).
    2. Age from 18-70. (70 with no other comorbiditeis)
    3. Their ASA score 1,2 or 3 (American Society of Anesthesia)
    4. General Anesthesia.
    5. Open inguinal hernia repair.
  • Exclusion criteria:

    1. All emergency inguinal hernia repair and recurrent hernia.
    2. Children and pregnant women.
    3. Patients having regional anesthesia. (Spinal/Local).
    4. Laparoscopic inguinal hernia.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Other

    Arm Label

    The experimental group will receive US guided nerve block

    The control group will receive usual infiltration

    Arm Description

    The experimental group will receive US guided nerve block by lidocaine before open inguinal hernia repair.

    The control group will receive usual infiltration by lidocaine before open inguinal hernia repair.

    Outcomes

    Primary Outcome Measures

    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Assessment of pain scale post operative, lower score mean a better outcome.
    Assessment of early mobilisation.
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Assessment of early mobilisation.
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Assessment of early mobilisation.
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Retain to driving (how many days between surgery and patient back to dive)
    When the patient back to drive his car? assessed by monitoring the patients postoperative and record when he started to drive the car again.
    Retain to work (how many days between surgery and patient back to his work)
    When the patient back to his work or usual activity? assessed by monitoring the patients postoperative and record when he started to work again.
    Length of hospital stay (in days).
    Length of hospital stay post open inguinal hernia repair ( how many days patient spend in the hospital postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Frequency of analgesia consumption postoperative.
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).

    Secondary Outcome Measures

    Full Information

    First Posted
    February 9, 2021
    Last Updated
    October 31, 2021
    Sponsor
    Imam Abdulrahman Bin Faisal University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04792164
    Brief Title
    Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.
    Official Title
    Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair: Randomised Control Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    December 1, 2021 (Anticipated)
    Primary Completion Date
    December 29, 2022 (Anticipated)
    Study Completion Date
    June 29, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Imam Abdulrahman Bin Faisal University

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No

    5. Study Description

    Brief Summary
    A hernia occurs when an organ 'like intestines' or fatty tissue protrude through a weak point in muscle or connective tissue and one of the most common types of hernia is inguinal. Inguinal hernia defined as a bulge in the inguinal region or scrotum, may be accompanied by dull or burning pain, which worsens by exercise or cough. There are 2 types of inguinal hernia: direct and indirect. Direct inguinal hernia occurs because of a defect or weakness in the transversalis fascia area of the Hesselbach triangle. On the other hand, the indirect inguinal hernia which is the most common inguinal hernia follows the tract of inguinal canal and result from a persistent processus vaginalis. Immediate pain after inguinal herniorrhaphy delays the ambulation which leads to delay in the hospital discharge. Besides that, is the chronic pain that affect 50% of patients which is an important issue that needs to be dealt with. Our aim of this study, is to compare between postoperative period in the patients who received US guided nerve block and in patients who received infiltration only before open inguinal hernia repair, and to show that pre-emptive local anaesthesia will result in better pain control, less postoperative complication, earlier mobilisation, earlier recovery and less analgesia consumption by patients.
    Detailed Description
    In this study our aim in detail is to: Asses the outcomes (early postoperative pain management in day case "day 1,2,3, 30 and 3 month and 6 month" , length of hospital stay, analgesia consumption، recovery to work, driving and usual activity) of the US guided nerve block in patients who underwent inguinal hernia repair comparing to patient who received only skin infiltration. Evaluate the advantages of the US guided nerve block in postoperative inguinal hernia repair patients. Demonstrate its compatibly as a one day procedure (less length of hospital stay), with earlier return to work and driving and recovery in general. Compare our result with other international studies result. Study in details: it is Randomised Control Trial, Double blinded (patients and recruiter), study will be conducted in King Fahd University Hospital, Khobar, Eastern Province, Saudi Arabia. It contains 2 Arms ,Two Parallel groups. The experimental group will receive US guided nerve block and the control group will receive usual infiltration. Lidocaine+ Marcaine will be used in both group with same concentration (1%+.25%). The random allocation will be done using simple random allocation with a help of the following software (random.org). Will compare the two groups regarding, a questionary with visual analogue will be distributed and data will be collected by recruiters regarding pain scale, length of hospital stay, return to work, return to driving and usual activity, and analgesia consumption post operative, all in day 1,2,3,4,30,3 month and 6 month post operatives (details in outcome section). We are expecting to have a reduction in pain score from severe to moderate, about 20% in experimental group, and reducing the length of hospital stay from 1-2 days to one day procedure. And reduction in consumption of Analgesia postoperative. our sample size will be 134 with a power of 80% and an effect size of 0.5, will include all patients who will have inguinal hernia repair and meet our inclusion criteria, in period of 12-18 months starting after obtaining of IRB approval. Inclusion criteria: Patients who underwent elective inguinal hernia repair (will consider the hernia size). Age from 18-70. Their ASA score 1,2 or 3 (American Society of Anesthesia) Operation under general anaesthesia. Open inguinal hernia repair. Exclusion criteria: All emergency inguinal hernia repair and recurrent hernia. Children and pregnant women. Patients having regional anaesthesia. (Spinal/Local). Laparoscopic inguinal hernia. Data Management and analysis plan: SPSS latest version will be used for data analysis. Summary statistic will be obtained as frequency, and percentage for qualitative data, and means, medians and standard deviations from continuous variables. Analysis will be done by epidemiologist and biostatistician. Ethical Considerations: Our study does not have any physical, psychological, social, legal, economic risk. The study will be reviewed by IRB, ethics committee; then the approval will be obtained. Written approval will be obtained from the patients prior to the procedure. Preemptive analgesia and infiltration are usually used in our practice and aim to compare.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Inguinal Hernia

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    2 Arms Arm1) The experimental group will receive US guided nerve block by Lidocaine+Marcaine concentration (1%+.25%). Arm2) The control group will receive usual infiltration by Lidocaine+Marcaine concentration (1%+.25%).
    Masking
    ParticipantOutcomes Assessor
    Masking Description
    Double blinded ( Patient and researcher recruiter)
    Allocation
    Randomized
    Enrollment
    136 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    The experimental group will receive US guided nerve block
    Arm Type
    Experimental
    Arm Description
    The experimental group will receive US guided nerve block by lidocaine before open inguinal hernia repair.
    Arm Title
    The control group will receive usual infiltration
    Arm Type
    Other
    Arm Description
    The control group will receive usual infiltration by lidocaine before open inguinal hernia repair.
    Intervention Type
    Procedure
    Intervention Name(s)
    Ultra sound guided nerve block
    Intervention Description
    Ultra sound guided nerve block by lidocaine before open inguinal hernia repair.
    Intervention Type
    Procedure
    Intervention Name(s)
    Usual infiltration
    Intervention Description
    Usual infiltration by lidocaine before open inguinal hernia repair.
    Primary Outcome Measure Information:
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    Day 1 postoperative.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    Day 2 postoperative.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    Day 3 postoperative.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    Day 4 postoperative.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    Day 30 postoperative.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    3 month postoperative for chronic pain.
    Title
    Pain Scale (from 1 to 10) 1 is the minimum and 10 the maximum pain severity.
    Description
    Assessment of pain scale post operative, lower score mean a better outcome.
    Time Frame
    6 month postoperative for chronic pain.
    Title
    Assessment of early mobilisation.
    Description
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Time Frame
    Day 1 postoperative period.
    Title
    Assessment of early mobilisation.
    Description
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Time Frame
    Day 2 postoperative period.
    Title
    Assessment of early mobilisation.
    Description
    When the patient started to mobilise? assessed by monitoring the patients postoperative and record when he started to mobilise.
    Time Frame
    Day 3 postoperative period.
    Title
    Retain to driving (how many days between surgery and patient back to dive)
    Description
    When the patient back to drive his car? assessed by monitoring the patients postoperative and record when he started to drive the car again.
    Time Frame
    Postoperative period up to 8 weeks.
    Title
    Retain to work (how many days between surgery and patient back to his work)
    Description
    When the patient back to his work or usual activity? assessed by monitoring the patients postoperative and record when he started to work again.
    Time Frame
    Postoperative period up to 8 weeks.
    Title
    Length of hospital stay (in days).
    Description
    Length of hospital stay post open inguinal hernia repair ( how many days patient spend in the hospital postoperative).
    Time Frame
    immediately after the surgery until patient discharged.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 1 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 2 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 3 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 4 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 5 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 6 postoperative.
    Title
    Frequency of analgesia consumption postoperative.
    Description
    Analgesia consumption by patient postoperative (How frequent patient taking analgesia postoperative).
    Time Frame
    Day 7 postoperative.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    70 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion criteria: Patients who underwent elective inguinal hernia repair (will consider the hernia size). Age from 18-70. (70 with no other comorbiditeis) Their ASA score 1,2 or 3 (American Society of Anesthesia) General Anesthesia. Open inguinal hernia repair. Exclusion criteria: All emergency inguinal hernia repair and recurrent hernia. Children and pregnant women. Patients having regional anesthesia. (Spinal/Local). Laparoscopic inguinal hernia.
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Nasser M Amer
    Phone
    00966 53 865 9290
    Email
    nmamer@iau.edu.sa

    12. IPD Sharing Statement

    Learn more about this trial

    Effect of Ultra-Sound Guided Pre-emptive Nerve Block on Post-operative Pain Following Open Inguinal Hernia Repair.

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